Skip to main content
PolicySpeak
← All files

EU consultation

Evaluation of the Biocidal Products Regulation

124 submissions from 121 organizations told the European Commission what they think about this file. Here is what each of them said, in their own words.

The Commission lists 282 submissions on this file. Shown here: the 124 from organizations. Not shown, by design: submissions from private individuals, which we never publish, and anything filed since our last weekly refresh.

Who showed up

94 submissions from industry — companies and their trade associations — against 15 from civil society: NGOs, consumer organizations, environmental groups and trade unions. That is 6.3 industry submissions for every one from civil society.

Industry 94Civil society 15Public authorities, academia, other 15

Groupings use the respondent type each organization selected when filing. Counting submissions, not organizations — a body that filed twice is counted twice.

What the room declares

42 of 121
in the EU Register
233
full-time lobbying staff
€29.9M+
declared costs a year
123
EP accreditations declared

Self-declared to the EU Transparency Register (snapshot 30 Aug 2026). The cost figure sums band floors, so the true total is higher.

The file, right now

The consultation closed on 5 Mar 2026 — it ran from 11 Dec 2025.

Policy area
Health & food (DG SANTE)
Where it stands
Awaiting adoption
Adoption expected
30 Sept 2027 · in 396 days

How it got here

  1. Call for evidence · evaluation5 Mar 2026
  2. Public consultation5 Mar 2026

Also on the Commission’s pipeline for this file, with no date recorded: Initiative planned, Report.

124 positions · showing 25

KO

Kosmetik- og hygiejnebranchen

· · filed 5 Mar 2026 · source

Cosmetics and hygiene industry, representing Danish manufacturers of disinfectants, welcomes the opportunity to comment on the ongoing Call for evidence regarding the evaluation of the BPR. The purpose of the BPR is to ensure a high level of protection of both human and animal health and the environment in addition to improving the functioning of the internal market.

Filed in Danish · English published by the European Commission

LinkedInX
LP

Laboratoire PAREVA

· · filed 5 Mar 2026 · source

The following points should be discussed to simplify the BPR, while aiming to reduce the growing ‎inequality between active substancesa result of delays in the Review Program and the introduction ‎of new regulatory requirements:‎ ‎(1)‎ Require MSCA to prioritize the assessment of Active Substance (AS) dossiers that have never ‎been evaluated.

LinkedInX
SR

Sagentia Regulatory (TSG)

· · filed 5 Mar 2026 · source

PDF

Consultation Response Evaluation of the Biocidal Products Regulation (BPR) 1 Introduction Sagentia Regulatory, formerly TSG Consulting, has been actively involved in the implementation of the EU Biocidal Products Regulation (BPR) since its introduction.

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
TG

THOR GmbH

· · filed 5 Mar 2026 · source

PDF

THOR is a global producer of speciality chemicals, delivering high-performance biocide, flame-retardant and personal-care solutions. Founded in England, we operate world-wide, enhancing the safety, durability and functionality of products across construction, coatings, hygiene, automotive, water treatment, personal care, textile sectors and more.

Filed in German · English published by the European Commission

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
AF

Andermatt France

· · filed 5 Mar 2026 · source

The presence of non-compliant biocidal products on the EU market raises significant concerns in terms of public health, environmental protection and the integrity of the regulatory framework established by the Biocidal Products Regulation (BPR). The BPR aims to ensure that biocidal products placed on the EU market meet strict safety, efficacy and risk assessment requirements.

Filed in French · English published by the European Commission

LinkedInX
LP

Laboratoire PAREVA

· · filed 5 Mar 2026 · source

Our proposal to simplify the BPR: ‎ ‎ – ‎ A single dossier only per biocidal Active Substance, ‎ regardless of the number of intended product ‎ types (pts) to be supported ‎ – Composition of such dossier: Only Part A is required (meeting the requirements of Annex II of the ‎ BPR). ‎ – Uniform application: The same rule applies to both new active substances and existing ones (under ‎ the Review Programme).

Filed in French · English published by the European Commission

LinkedInX
GN

Glastuinbouw Nederland

· · filed 5 Mar 2026 · source

PDF

European controlled environment agriculture (CEA) is among the most advanced and resource-efficient horticultural production systems in the world. High-tech CEA allows growers to grow fruits, vegetables, flowers, and plants with efficient use of water, nutrients, and energy, while minimising emissions to the environment.

LinkedInX
WE

Women Engage for a Common Future, WECF

· · filed 5 Mar 2026 · source

Women Engage for a Common Future (WECF) welcomes the opportunity to contribute to the evaluation of the Biocidal Products Regulation (BPR). Biocidal products are designed to control harmful organisms and therefore inherently pose risks to human health and the environment.

LinkedInX
PI

PPG Industries Inc.

· · filed 5 Mar 2026 · source

PDF

We would like to thank EC for the opportunity to voice our company concerns and the opportunity to contribute to the call for evidence on the BPR. As mentioned in the introduction to this consultation, biocidal products (biocides) have the important role to help to control unwanted organisms that are harmful to human or animal health or to the environment, or that cause damage to materials or human activities.

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
L

Liphatech

· · filed 5 Mar 2026 · source

Our company has been operating under the Biocidal Products Directive and now the BPR. While we fully support the objectives of protecting human/animal health, the environment and the internal market, our operational experience shows that the current regulatory framework is no longer sustainable for organisations nor for users, including professionals, who depend on these products.

LinkedInX
DG

Deutsche Gesellschaft für das Badewesen e.V.

· · filed 5 Mar 2026 · source

PDF

Europäische Kommission Generaldirektion Gesundheit und Lebensmittelsicherheit (SANTE) Referat E4 – Pestizide und Biozide Frau [name removed] – per Mail – Regelwerk und Beratung Ansprechpartner: [name removed] Telefon: [phone removed] [email removed] www.dgfdb.de 29.11.2022 Verordnung über Biozidprodukte – Bewertung Sehr geehrte Frau Bitterhof, sehr geehrte Damen und Herren, die Deutsche Gesellschaft für das…

Filed in German · English published by the European Commission

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
RT

Rütgers Organics GmbH

· · filed 5 Mar 2026 · source

PDF

Statement for the consultation on evaluation of the EU Biocidal Products Regulation (BPR). Wood preservative manufacturer Rütgers Organics GmbH appreciates the opportunity to contribute to the process of refinement of the EU regulation No. 528/2012 (BPR).

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
MD

Ministero della salute

· · filed 5 Mar 2026 · source

PDF

IT COMMENTS ON THE REVISION OF EU BIOCIDAL PRODUCTS REGULATION NO. 528/2012 Ar cle 5 Exclusion criteria Ar cle 5 should be updated taking into account the new CLP hazard classes with harmonised classifica on. EXPLANATION For ac ve substances that already have a CLP harmonised classifica on, their hazard does not need to be reassessed.

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
E

EURODOM

· · filed 5 Mar 2026 · source

PDF

Contribution Eurodom à l’évaluation sur le règlement biocides 528/2012 Nous proposons d’introduire (dans le règlement 528/2012, ses actes d’exécution et/ou les lignes directrices d’application) une clarification et une voie d’autorisation permettant, à titre strictement encadré, l’utilisation de rodenticides biocides en milieux agricoles lorsque les finalités relèvent de la santé publique (prévention d’une zoonose)…

Filed in French · English published by the European Commission

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
IT

I-Tech AB

· · filed 5 Mar 2026 · source

PDF

Contribution to the Evaluation of the Biocidal Products Regulation (EU) No 528/2012 I-Tech AB (“I-Tech”) is a Swedish biotechnology company specialising in marine antifouling solutions. A long-time recipient of EU funding, I-Tech is the developer of Selektope® (medetomidine), an innovative biocidal active substance currently approved under the BPR.

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
WE

WTR Europe GmbH

· · filed 5 Mar 2026 · source

PDF

WTR is a SME and a relative newcomer to the BPR. While the BPR has successfully established a high level of protection for human health and the environment, its implementation has inadvertently created a regulatory environment where "data protection" is frequently used as a tool for "market protection".

LinkedInX
A

anefp

· · filed 5 Mar 2026 · source

PDF

Autocuidado de la Salud Ref. Ares(2026)2451026 - 05/03/2026 anefp contributions to the Public Consultation on Regulation (EU) 528/2012 concerning the making available on the market and use of biocidal products anefp welcomes the ongoing revision of Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products (BPR) and considers it a valuable opportunity to incorporate into…

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
PB

Platform Biociden

· · filed 5 Mar 2026 · source

PDF

Platform Biociden, the Dutch trade association representing the biocides value chain, welcomes the European Commissions evaluation of the Biocidal Products Regulation (BPR). We believe that its current implementation is no longer fit for purpose in terms of competitiveness, predictability and proportionality and requires evaluation and reform.

LinkedInX
CF

Center for Wild Animal Welfare

· · filed 5 Mar 2026 · source

PDF

Ares(2026)2450779 CWAW Policy Briefing: Wild AnimalRef. Welfare in the BPR - 05/03/2026 Wild Animal Welfare in the Biocidal Products Regulation Evidence submitted to the Biocidal Products Regulation evaluation, March 2026 The Center for Wild Animal Welfare (CWAW) is a non-profit organisation that aims to improve the lives of wild animals through government policy.

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
PA

Pesticide Action Network (PAN) Europe

· · filed 5 Mar 2026 · source

PDF

PAN Europe welcomes the opportunity to contribute to the evaluation of the Biocidal Products Regulation (BPR) and emphasises the importance of a strong, science-based framework to protect human health, animals, and the environment. Biocidal products are inherently hazardous, and their use requires high regulatory standards to ensure safety. However, significant challenges remain in the implementation of the BPR.

LinkedInX
GN

Générations Futures

· · filed 5 Mar 2026 · source

PDF

Ares(2026)2450053 - 05/03/2026 Biocidal products regulation evaluation - 05 Ref. March 2023 “The purpose of this Regulation is to improve the free movement of biocidal products within the Union while ensuring a high level of protection of both human and animal health and the environment. Particular attention should be paid to the protection of vulnerable groups, such as pregnant women and children.

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
CE

CITREFINE EU LIMITED

· · filed 5 Mar 2026 · source

PDF

Our company is an SME that has supported an active substance under the BPD and continues to do so under the BPR. We believe the aims of the BPR are still relevant but that there have been, and continue to be, areas where significant improvements could be made to the cost effectiveness and efficiency by ensuring greater clarity, restricting ad hoc changes and ensuring that robust data underpins any alterations.

LinkedInX
AT

Alliance to Save Our Antibiotics

· · filed 5 Mar 2026 · source

PDF

Alliance to Save Our Antibiotics feedback on Biocides Products Regulation, March 2025 The Alliance to Save Our Antibiotics believes that much tighter regulation of biocide use is needed in the EU, to minimise the contribution that these chemicals make to the rise of antimicrobial resistance (AMR).

Opening of the attached position paper · the full paper is on the Commission’s record (source link above)

LinkedInX
PA

Pestizid Aktions-Netzwerk e.V. (PAN Germany)

· · filed 5 Mar 2026 · source

PDF

The Pesticide Action Network (PAN) Germany welcomes the opportunity to comment on the Regulation on Biocidal Products Regulation (EU) No 528/2012 (BPR) and its evaluation. From an environmental and consumer protection perspective, the BPR is a very important and useful legal instrument for establishing uniform provisions to regulate the placing on the market and use of biocidal products and biocidal treated articles…

LinkedInX
BG

BIOFA GmbH

· · filed 5 Mar 2026 · source

PDF

Non-compliant biocidal products put EU consumers health at risk.The BPR ensures that biocidal products placed on the EU market meet stringent safety and efficacy standards, minimizing risks to human health and the environment: Non-compliant products circumvent regulatory scrutiny, posing potential health hazards due to unknown toxicity, inadequate risk assessments, and misleading safety claims.

LinkedInX
Take the dataCSV — all 124 submissionsJSONFull text, not the excerpt. Free to cite.Search every submission →

Follow this file

Get an email when a new organization files a position here: one email on Tuesdays, only when there is something new. Free.

We use your email for updates on this file, and PolicySpeak may contact you about the product. Unsubscribe in one click. Privacy policy.

Method. Every quote is verbatim from the organization’s own submission to the European Commission, trimmed to its opening passage and never summarized by a model. Where a submission was filed in another EU language we show the English text the European Commission publishes alongside it, labeled on the quote; the original is one click away at the source. Groupings use the respondent type the organization itself selected when filing. We deliberately do not label anyone “supportive” or “opposed” — you read what they wrote and draw your own conclusion. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.